Canonical Allele Identifier: CA2502961004

Gene: DNMT3B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32805519_32805520insG , CM000682.2:g.32805519_32805520insG	GRCh38
NC_000020.10:g.31393325_31393326insG , CM000682.1:g.31393325_31393326insG	GRCh37
NC_000020.9:g.30856986_30856987insG	NCBI36
NG_007290.1:g.48135_48136insG , LRG_56:g.48135_48136insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1252+112_*1252+113insG	ENSP00000512497.1:n.*1252+112_*1252+113insG
ENST00000696232.1:c.2232-2243_2232-2242insG	ENSP00000512498.1:n.2232-2243_2232-2242insG
ENST00000696233.1:c.*975-2243_*975-2242insG	ENSP00000512499.1:n.*975-2243_*975-2242insG
ENST00000696238.1:c.*1044+112_*1044+113insG	ENSP00000512502.1:n.*1044+112_*1044+113insG
ENST00000696239.1:c.2082+112_2082+113insG	ENSP00000512503.1:n.2082+112_2082+113insG
ENST00000696245.1:n.327-690_327-689insG
ENST00000201963.3:c.2277+112_2277+113insG	ENSP00000201963.3:n.2277+112_2277+113insG
ENST00000328111.6:c.2301+112_2301+113insG MANE Select	ENSP00000328547.2:n.2301+112_2301+113insG
ENST00000348286.6:c.2172-2243_2172-2242insG	ENSP00000337764.2:n.2172-2243_2172-2242insG
ENST00000353855.6:c.2241+112_2241+113insG	ENSP00000313397.4:n.2241+112_2241+113insG
ENST00000443239.7:c.2046-2243_2046-2242insG	ENSP00000403169.2:n.2046-2243_2046-2242insG
ENST00000456297.6:c.1944-2243_1944-2242insG	ENSP00000412305.1:n.1944-2243_1944-2242insG
NM_001207055.1:c.2046-2243_2046-2242insG	NP_001193984.1:n.2046-2243_2046-2242insG
NM_001207056.1:c.1944-2243_1944-2242insG	NP_001193985.1:n.1944-2243_1944-2242insG
NM_006892.3:c.2301+112_2301+113insG , LRG_56t1:c.2301+112_2301+113insG	NP_008823.1:n.2301+112_2301+113insG
NM_175848.1:c.2241+112_2241+113insG	NP_787044.1:n.2241+112_2241+113insG
NM_175849.1:c.2172-2243_2172-2242insG	NP_787045.1:n.2172-2243_2172-2242insG
NM_175850.2:c.2277+112_2277+113insG	NP_787046.1:n.2277+112_2277+113insG
XM_011528653.1:c.2208-2243_2208-2242insG	XP_011526955.1:n.2208-2243_2208-2242insG
XM_011528654.1:c.2082-2243_2082-2242insG	XP_011526956.1:n.2082-2243_2082-2242insG
XR_936510.1:n.2268+112_2268+113insG
XR_936511.1:n.2199-2243_2199-2242insG
XR_936512.1:n.2143+112_2143+113insG
XM_011528653.2:c.2208-2243_2208-2242insG	XP_011526955.1:n.2208-2243_2208-2242insG
XM_011528654.2:c.2082-2243_2082-2242insG	XP_011526956.1:n.2082-2243_2082-2242insG
XR_936510.2:n.2279+112_2279+113insG
XR_936511.2:n.2210-2243_2210-2242insG
XR_936512.2:n.2155+112_2155+113insG
NM_001207055.2:c.2046-2243_2046-2242insG	NP_001193984.1:n.2046-2243_2046-2242insG
NM_001207056.2:c.1944-2243_1944-2242insG	NP_001193985.1:n.1944-2243_1944-2242insG
NM_006892.4:c.2301+112_2301+113insG MANE Select	NP_008823.1:n.2301+112_2301+113insG
NM_175848.2:c.2241+112_2241+113insG	NP_787044.1:n.2241+112_2241+113insG
NM_175849.2:c.2172-2243_2172-2242insG	NP_787045.1:n.2172-2243_2172-2242insG
NM_175850.3:c.2277+112_2277+113insG	NP_787046.1:n.2277+112_2277+113insG